Terpenoid chemistry. XV. 1,5-Dimethylcyclodeca-1,5,7-triene, the precursor of geijerene in Geijera parviflora (Lindley)

Authors:
  • RJRvj Jones
    Rvj Jones
  • SUSutherland
    Sutherland
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Abstract
Geijera parviflora leaves which yield geijerene when worked up under the usual conditions of steam-distillation and fractional distillation have been found to contain a new hydrocarbon, Cl2H18 (pregeijerene), and only a trace of geijerene. The structure of pregeijerene has been shown by degradative and spectral examination to be 1,5-dimethylcyclodeca-1,5,7-triene, the disubstituted double bond having a cis configuration. The hydrocarbon forms a crystalline adduct with silver nitrate and rearranges thermally to yield geijerene.